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Details of MMAB gene in Homo sapiens
IDs |
Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
| MMAB | --- | Q96EY8 | MMAB_HUMAN | 326625 | ENSG00000139428 | Cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial | SPROT |
Disease |
Disease |
OMIM id |
Methylmalonic aciduria type cblB (MMAB) [MIM:251110]: A disorder of methylmalonate and cobalamin metabolism due to defective synthesis of adenosylcobalamin. Note=The disease is caused by mutations affecting the gene represented in this entry. |
251110 |
Orthologs in other species |
M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
Mmab | --- | mmab-1 | Sp-Mmab |